Introduction to Drug Pharmacokinetics in the Critically Ill Patient

被引:183
作者
Smith, Brian S. [1 ]
Yogaratnam, Dinesh [1 ]
Levasseur-Franklin, Kimberly E. [2 ]
Forni, Allison [3 ]
Fong, Jeffrey [1 ,4 ]
机构
[1] UMass Mem Med Ctr, Worcester, MA 01655 USA
[2] NW Mem Hosp, Chicago, IL 60611 USA
[3] Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Massachusetts Coll Pharm & Hlth Sci, Worcester, MA USA
关键词
RENAL REPLACEMENT THERAPY; PLASMA-PROTEIN BINDING; INTENSIVE-CARE; PHARMACODYNAMICS; EVENTS; TRAUMA; METABOLISM; PHENYTOIN; FAILURE; BIOAVAILABILITY;
D O I
10.1378/chest.11-1396
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Despite regular use of drugs for critically ill patients, overall data are limited regarding the impact of critical illness on pharmacokinetics (PK). Designing safe and effective drug regimens for patients with critical illness requires an understanding of PK. This article reviews general principles of PK, including absorption, distribution, metabolism, and elimination, and how critical illness can influence these parameters. In the area of drug absorption, we discuss the impact of vasopressor use, delayed gastric emptying and feeding tubes, and nutrient interactions. On the topic of drug distribution, we review fluid resuscitation, alterations in plasma protein binding, and tissue perfusion. With drug metabolism, we discuss hepatic enzyme activity, protein binding, and hepatic blood flow. Finally, we review drug elimination in the critically ill patient and discuss the impact of augmented renal clearance and acute kidney injury on drug therapies. In each section, we highlight select literature reviewing the PK impact of these conditions on a drug PK profile and, where appropriate, provide general suggestions for clinicians on how to modify drug regimens to manage PK challenges. CHEST 2012; 141(5):1327-1336
引用
收藏
页码:1327 / 1336
页数:10
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